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Twist exome capture allows for lower average sequence coverage in clinical exome sequencing
Authors :
Yaldiz, Burcu Kucuk, Erdi Hampstead, Juliet Hofste, Tom Pfundt, Rolph Corominas Galbany, Jordi Rinne, Tuula Yntema, Helger G. Hoischen, Alexander Nelen, Marcel Gilissen, Christian consortium, Solve-R. D. Riess, Olaf Haack, Tobias B. Graessner, Holm Zurek, Birte Ellwanger, Kornelia Ossowski, Stephan Demidov, German Sturm, Marc Schulze-Hentrich, Julia M. Schüle, Rebecca Xu, Jishu Kessler, Christoph Wayand, Melanie Synofzik, Matthis Wilke, Carlo Traschütz, Andreas Schöls, Ludger Hengel, Holger Lerche, Holger Kegele, Josua Heutink, Peter Brunner, Han Scheffer, Hans Hoogerbrugge, Nicoline Hoen, Peter A. C. T Vissers, Lisenka E. L. M. Steyaert, Wouter Sablauskas, Karolis de Voer, Richarda M. Kamsteeg, Erik-Jan van de Warrenburg, Bart van Os, Nienke te Paske, Iris Janssen, Erik de Boer, Elke Steehouwer, Marloes Kleefstra, Tjitske Brookes, Anthony J. Veal, Colin Gibson, Spencer Maddi, Vatsalya Mehtarizadeh, Mehdi Riaz, Umar Warren, Greg Dizjikan, Farid Yavari Shorter, Thomas Töpf, Ana Straub, Volker Bettolo, Chiara Marini Manera, Jordi Diaz Hambleton, Sophie Engelhardt, Karin Clayton-Smith, Jill Banka, Siddharth Alexander, Elizabeth Jackson, Adam Faivre, Laurence Thauvin, Christel Vitobello, Antonio Denommé-Pichon, Anne-Sophie Duffourd, Yannis Bruel, Ange-Line Peyron, Christine Pélissier, Aurore Beltran, Sergi Gut, Ivo Glynne Laurie, Steven Piscia, Davide Matalonga, Leslie Papakonstantinou, Anastasios Bullich, Gemma Corvo, Alberto Fernandez-Callejo, Marcos Hernández, Carles Picó, Daniel Paramonov, Ida Lochmüller, Hanns Gumus, Gulcin Bros-Facer, Virginie Rath, Ana Hanauer, Marc Lagorce, David Hongnat, Oscar Chahdil, Maroua Lebreton, Emeline Stevanin, Giovanni Durr, Alexandra Davoine, Claire-Sophie Guillot-Noel, Léna Heinzmann, Anna Coarelli, Giulia Bonne, Gisèle Evangelista, Teresinha Allamand, Valérie Nelson, Isabelle Yaou, Rabah Ben Metay, Corinne Eymard, Bruno Cohen, Enzo Atalaia, Antonio Stojkovic, Tanya Macek, Milan Turnovec, Marek Thomasová, Dana Kremliková, Radka Pourová Franková, Vera Havlovicová, Markéta Lišková, Petra Doležalová, Pavla Parkinson, Helen Keane, Thomas Freeberg, Mallory Thomas, Coline Spalding, Dylan Robinson, Peter Danis, Daniel Robert, Glenn Costa, Alessia Patch, Christine Hanna, Mike Houlden, Henry Reilly, Mary Vandrovcova, Jana Efthymiou, Stephanie Morsy, Heba Cali, Elisa Magrinelli, Francesca Sisodiya, Sanjay M. Rohrer, Jonathan Muntoni, Francesco Zaharieva, Irina Sarkozy, Anna Timmerman, Vincent Baets, Jonathan de Vries, Geert De Winter, Jonathan Beijer, Danique de Jonghe, Peter Van de Vondel, Liedewei De Ridder, Willem Weckhuysen, Sarah Nigro, Vincenzo Mutarelli, Margherita Morleo, Manuela Pinelli, Michele Varavallo, Alessandra Banfi, Sandro Torella, Annalaura Musacchia, Francesco Piluso, Giulio Ferlini, Alessandra Selvatici, Rita Gualandi, Francesca Bigoni, Stefania Rossi, Rachele Neri, Marcella Aretz, Stefan Spier, Isabel Sommer, Anna Katharina Peters, Sophia Oliveira, Carla Pelaez, Jose Garcia Matos, Ana Rita José, Celina São Ferreira, Marta Gullo, Irene Fernandes, Susana Garrido, Luzia Ferreira, Pedro Carneiro, Fátima Swertz, Morris A. Johansson, Lennart van der Velde, Joeri K. van der Vries, Gerben Neerincx, Pieter B. Ruvolo, David Abbott, Kristin M. Frederikse, Wilhemina Skerstjens Zonneveld-Huijssoon, Eveline Roelofs-Prins, Dieuwke van Gijn, Marielle Köhler, Sebastian Metcalfe, Alison Verloes, Alain Drunat, Séverine Heron, Delphine Mignot, Cyril Keren, Boris de Sainte Agathe, Jean-Madeleine Rooryck, Caroline Lacombe, Didier Trimouille, Aurelien De la Paz, Manuel Posada Sánchez, Eva Bermejo Martín, Estrella López Delgado, Beatriz Martínez de la Rosa, F. Javier Alonso García Ciolfi, Andrea Dallapiccola, Bruno Pizzi, Simone Radio, Francesca Clementina Tartaglia, Marco Renieri, Alessandra Furini, Simone Fallerini, Chiara Benetti, Elisa Balicza, Peter Molnar, Maria Judit Maver, Ales Peterlin, Borut Münchau, Alexander Lohmann, Katja Herzog, Rebecca Pauly, Martje Macaya, Alfons Cazurro-Gutiérrez, Ana Pérez-Dueñas, Belén Munell, Francina Jarava, Clara Franco Masó, Laura Batlle Marcé-Grau, Anna Colobran, Roger Osorio, Andrés Nascimento de Benito, Daniel Natera Thompson, Rachel Polavarapu, Kiran Grimbacher, Bodo Beeson, David Cossins, Judith Hackman, Peter Johari, Mridul Savarese, Marco Udd, Bjarne Horvath, Rita Chinnery, Patrick F. Ratnaike, Thiloka Gao, Fei Schon, Katherine Capella, Gabriel Valle, Laura Holinski-Feder, Elke Laner, Andreas Steinke-Lange, Verena Schröck, Evelin Rump, Andreas Başak, Ayşe Nazlı Hemelsoet, Dimitri Dermaut, Bart Schuermans, Nika Poppe, Bruce Verdin, Hannah Mei, Davide Vetro, Annalisa Balestrini, Simona Guerrini, Renzo Claeys, Kristl Santen, Gijs W. E. Bijlsma, Emilia K. Hoffer, Mariette J. V. Ruivenkamp, Claudia A. L. Boztug, Kaan Haimel, Matthias Maystadt, Isabelle Cordts, Isabelle Deschauer, Marcus Zaganas, Ioannis Kokosali, Evgenia Lambros, Mathioudakis Evangeliou, Athanasios Spilioti, Martha Kapaki, Elisabeth Bourbouli, Mara Striano, Pasquale Zara, Federico Riva, Antonella Iacomino, Michele Uva, Paolo Scala, Marcello Scudieri, Paolo Cilio, Maria-Roberta Carpancea, Evelina Depondt, Chantal Lederer, Damien Sznajer, Yves Duerinckx, Sarah Mary, Sandrine Depienne, Christel Roos, Andreas May, Patrick Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) [research center]
Publication Year :
2023
Abstract
Background Exome and genome sequencing are the predominant techniques in the diagnosis and research of genetic disorders. Sufficient, uniform and reproducible/consistent sequence coverage is a main determinant for the sensitivity to detect single-nucleotide (SNVs) and copy number variants (CNVs). Here we compared the ability to obtain comprehensive exome coverage for recent exome capture kits and genome sequencing techniques. Results We compared three different widely used enrichment kits (Agilent SureSelect Human All Exon V5, Agilent SureSelect Human All Exon V7 and Twist Bioscience) as well as short-read and long-read WGS. We show that the Twist exome capture significantly improves complete coverage and coverage uniformity across coding regions compared to other exome capture kits. Twist performance is comparable to that of both short- and long-read whole genome sequencing. Additionally, we show that even at a reduced average coverage of 70× there is only minimal loss in sensitivity for SNV and CNV detection. Conclusion We conclude that exome sequencing with Twist represents a significant improvement and could be performed at lower sequence coverage compared to other exome capture techniques.
Details
Language :
English
Database :
OpenAIRE
Accession number :
edsair.od......2658..bb64e033e586f26becdded7d81c9709e